4-Methylmorpholine → HCID 57980172, compound
Reaction equation
[Na+].[C:2]([C:5]1[CH:6]=[CH:7][C:8]([C:11]2[CH:19]=[CH:18][C:14]([C:15]([O-:17])=O)=[CH:13][CH:12]=2)=[N:9][CH:10]=1)(=[O:4])[CH3:3].CN1CCOCC1.ClC1N=C(OC)N=C(OC)N=1.[NH:38]1[CH2:42][CH2:41][CH2:40][C@H:39]1[CH2:43][N:44]1[CH2:48][CH2:47][CH2:46][CH2:45]1>ClCCl>[N:44]1([CH2:43][C@@H:39]2[CH2:40][CH2:41][CH2:42][N:38]2[C:15]([C:14]2[CH:13]=[CH:12][C:11]([C:8]3[N:9]=[CH:10][C:5]([C:2](=[O:4])[CH3:3])=[CH:6][CH:7]=3)=[CH:19][CH:18]=2)=[O:17])[CH2:48][CH2:47][CH2:46][CH2:45]1Participants
Procedure
Procedure W′: To a stirring solution of 4-(5-acetyl-pyridin-2-yl)-benzoic acid sodium salt (1.0 mmol) and n-methyl morpholine (1.0 mmol) in dichloromethane (0.10M) in a 0° C. ice bath, add 2-chloro-4,6-dimethoxy-1,3,5-triazine (1.0 mmol). Remove the ice bath and stir for 45 minutes. After this time, add (S)-(+)-1-(2-pyrrolidinylmethyl)pyrrolidine (1.0 mmol) and stir at room temperature for three hours. After this time, wash the reaction with saturated aqueous sodium bicarbonate while extracting with 10% isopropanol/dichloromethane (3×). Dry the organic layer with sodium sulfate, filter and concentrate in vacuo. Purify the title compound via chromatography eluting with 2M ammonia in methanol and dichloromethane. MS (m/e): 378.3 (M+1)
Workup
- customRemove the ice bath
- stirringstir at room temperature for three hours
- washAfter this time, wash
- customthe reaction with saturated aqueous sodium bicarbonate
- extractionwhile extracting with 10% isopropanol/dichloromethane (3×)
- dry with materialDry the organic layer with sodium sulfate
- filtrationfilter
- concentrationconcentrate in vacuo
- customPurify the title compound via chromatography
- washeluting with 2M ammonia in methanol and dichloromethane
Sources & evidence
- ORD record
- ord-d9e3643d3d1245918c717f00e186fad8
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08008301B2
Reaction notes
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